Director Biostatistics

Bristol Myers Squibb

Madison, NJ, United States
Base: $218,740 - $265,060; bonus/equity: + incenti...
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Clinical trials
Drug development
Regulatory approval
** Bristol Myers Squibb is seeking a Director of Biostatistics to lead cross-functional teams in the design and execution of clinical trials aimed at transforming patient lives through innovative therapies. The ideal candidate will have extensive experience in biostatistics, clinical trials, and drug development, coupled with strong leadership and communication skills. **

Job Summary

  • Drives innovative and efficient study design to support regulatory approval, medical research, and market access.
  • Provides guidance and management to statisticians to ensure high quality and timely deliverables, managing resources and setting priorities.
  • Contributes to Clinical Development Plans, leads submission activities, and defends complex statistical solutions to regulatory bodies.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Director of Biostatistics to lead cross-functional teams in the design and execution of clinical trials aimed at transforming patient lives through innovative therapies. The ideal candidate will have extensive experience in biostatistics, clinical trials, and drug development, coupled with strong leadership and communication skills. **

Salary

Base: $218,740 - $265,060; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Paid Time Off

Skills & Requirements

Must-have

  • clinical trials
  • drug development
  • regulatory approval
  • statistical analysis
  • SAS, R or Python proficiency

Nice-to-have

  • scientific and strategic partner
  • human touch to every treatment
  • inclusive culture
  • work-life balance

Key Requirements

  • PhD (9+ years) or MS (11+ years) in statistics or biostatistics
  • Clinical trials, drug development, pharmaceutical industry or healthcare experience
  • Proficiency in scientific computing/programming (SAS, R or Python)
  • Experience in preparing for global regulatory agency interactions
  • At least 3 years management experience preferred

Work Rights

Not specified

Tailored Resume

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